TY - JOUR
T1 - Association between vitamin K and the metabolic syndrome
T2 - A 10-year follow-up study in adults
AU - Dam, Veerle
AU - Dalmeijer, Geertje W.
AU - Vermeer, Cees
AU - Drummen, Nadja E.
AU - Knapen, Marjo H.
AU - Van Der Schouw, Yvonne T.
AU - Beulens, Joline W.
PY - 2015/6/1
Y1 - 2015/6/1
N2 - Context: The Metabolic Syndrome (MetS) is a cluster of metabolic abnormalities and is associated with increased risk of diabetes and cardiovascular diseases. Phylloquinone, menaquinones, and vitamin K status are associated with several components of MetS, but the association with MetS has hardly been studied to date. Objective: This study aimed to examine whether the intake and/or status of vitamin K is associated with MetS and its components. Design: This study comprised two cohorts, one of 402 women and one of 400 men (age 40-80 y). At followup 625 participants were still alive and willing to participate. Data were analyzed both cross sectionally and longitudinally with Poisson and linear regression adjusted for multiple con-founders. Baseline phylloquinone/menaquinone intakes were measured with a validated food frequency questionnaire and vitamin K status with serum desphospho-uncarborxylated matrix-Gla protein level. Results: At baseline 270 (34.5%) participants had MetS and 171 (35.7%) at followup. Cross sectionally, high menaquinones intakes were associated (Ptrend ô .08) with a lower prevalence of MetS with a prevalence ratio (PR) of 0.74 (95% confidence interval [CI], 0.54-1.03) for the highest vs the lowest tertile. At followup, the highest tertiles of menaquinones intake (PR = 0.62; 95% CI, 0.40-0.95) and vitamin K status (PR =; 0.57; 95% CI, 0.38-0.87) were associated (Ptrend = .01) with a lower occurrence of MetS. These associations were mainly driven by relations with lower triacylglycerol concentrations for menaquinones and lower waist circumference for vitamin K status. Phylloquinone intake was not associated with MetS prevalence. Conclusions: This study shows that a high intake of menaquinones and high vitamin K status are associated with a lower occurrence of MetS.
AB - Context: The Metabolic Syndrome (MetS) is a cluster of metabolic abnormalities and is associated with increased risk of diabetes and cardiovascular diseases. Phylloquinone, menaquinones, and vitamin K status are associated with several components of MetS, but the association with MetS has hardly been studied to date. Objective: This study aimed to examine whether the intake and/or status of vitamin K is associated with MetS and its components. Design: This study comprised two cohorts, one of 402 women and one of 400 men (age 40-80 y). At followup 625 participants were still alive and willing to participate. Data were analyzed both cross sectionally and longitudinally with Poisson and linear regression adjusted for multiple con-founders. Baseline phylloquinone/menaquinone intakes were measured with a validated food frequency questionnaire and vitamin K status with serum desphospho-uncarborxylated matrix-Gla protein level. Results: At baseline 270 (34.5%) participants had MetS and 171 (35.7%) at followup. Cross sectionally, high menaquinones intakes were associated (Ptrend ô .08) with a lower prevalence of MetS with a prevalence ratio (PR) of 0.74 (95% confidence interval [CI], 0.54-1.03) for the highest vs the lowest tertile. At followup, the highest tertiles of menaquinones intake (PR = 0.62; 95% CI, 0.40-0.95) and vitamin K status (PR =; 0.57; 95% CI, 0.38-0.87) were associated (Ptrend = .01) with a lower occurrence of MetS. These associations were mainly driven by relations with lower triacylglycerol concentrations for menaquinones and lower waist circumference for vitamin K status. Phylloquinone intake was not associated with MetS prevalence. Conclusions: This study shows that a high intake of menaquinones and high vitamin K status are associated with a lower occurrence of MetS.
UR - http://www.scopus.com/inward/record.url?scp=84930803579&partnerID=8YFLogxK
U2 - https://doi.org/10.1210/jc.2014-4449
DO - https://doi.org/10.1210/jc.2014-4449
M3 - Article
C2 - 25835288
SN - 0021-972X
VL - 100
SP - 2472
EP - 2479
JO - Journal of clinical endocrinology and metabolism
JF - Journal of clinical endocrinology and metabolism
IS - 6
ER -